{{Rsnum
|rsid=1046934
|Gene=TSEN15
|Chromosome=1
|position=184054395
|Orientation=plus
|GMAF=0.3214
|Gene_s=TSEN15
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 39.8 | 49.6 | 10.6
| HCB | 33.6 | 47.4 | 19.0
| JPT | 22.1 | 60.2 | 17.7
| YRI | 81.0 | 17.7 | 1.4
| ASW | 63.2 | 35.1 | 1.8
| CHB | 33.6 | 47.4 | 19.0
| CHD | 27.5 | 51.4 | 21.1
| GIH | 35.6 | 48.5 | 15.8
| LWK | 72.7 | 26.4 | 0.9
| MEX | 43.1 | 43.1 | 13.8
| MKK | 75.6 | 23.7 | 0.6
| TSI | 53.9 | 40.2 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=20881960
  |Trait=Height
  |Title=Hundreds of variants clustered in genomic loci and biological pathways affect human height.
  |RiskAllele=A
  |Pval=2E-31
  |OR=.04
  |ORtxt=[NR] unit decrease
  |OA=1
}}

{{PMID Auto
|PMID=19474294
|Title=Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
|OA=1
}}

{{PMID Auto
|PMID=24944287
|Title=Genetic Variants Related to Height and Risk of Atrial Fibrillation: The Cardiovascular Health Study
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}